600 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EFH-25
FDA UDI
BIOTRONIK SE & Co. KG·04035479144852·
EFH-16
FDA UDI
BIOTRONIK SE & Co. KG·04035479144821·
EFH-30
FDA UDI
BIOTRONIK SE & Co. KG·04035479144890·
EFH-7F-W
FDA UDI
BIOTRONIK SE & Co. KG·04035479145323·
EFH-8F-W
FDA UDI
BIOTRONIK SE & Co. KG·04035479145330·
EFH-6F-W
FDA UDI
BIOTRONIK SE & Co. KG·04035479157838·
EFH-6F-W
FDA UDI
BIOTRONIK SE & Co. KG·04035479157821·
SELOX ST 60
FDA Adverse Event
Malfunction
·BIOTRONIK GMBH AND CO.·Product code DTB·June 4, 2008
BELOS DR
FDA Adverse Event
Other
·BIOTRONIK, GMBH AND CO.·Product code LWS·March 2, 2006
SELOX SR 53
FDA Adverse Event
Malfunction
·BIOTRONIK GMBH AND CO.·Product code DTB·December 4, 2008
SELOX SR 60
FDA Adverse Event
Malfunction
·BIOTRONIK GMBH AND CO.·Product code DTB·June 13, 2008
KENTROX RV-S 65
FDA Adverse Event
Malfunction
·BIOTRONIK GMBH AND CO.·Product code LWS·June 13, 2008
LINOX TD 65/16
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code LWS·September 24, 2007
ELOX 45-BP, MODEL 330 132, EFH-27, MODEL 331 549, EXTENSION TOOL, MODEL 331 668
FDA 510(k)
FDA Class 3
·Cardiovascular
SETROX S 45
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVN·April 3, 2014
ABBOTT VASCULAR PERCLOSE PROGLIUDE
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code MGB·October 31, 2016
HENRY SCHEIN PRESSURE INDICATING PASTE
FDA Adverse Event
Injury
·DENTSPLY CAULK·Product code EFH·May 30, 2014
OCCLUDE ARTICULATION SPRAY
FDA Adverse Event
Injury
·PASCAL CO., INC.·Product code EFH·May 22, 2012
HYDENT ARTICULATION PASTE
FDA Adverse Event
PASCAL COMPANY, INC.·Product code EFH·July 21, 2015
HYDENT ARTICULATION PASTE
FDA Adverse Event
Injury
·PASCAL CO., INC.·Product code EFH·December 7, 2011